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Catalog Number:
39088
CAS Number:
543-20-4
Chlorure de succinyle
Purity:
≥ 95 % (dosage par titration)
Synonym(s):
Dichlorure de butanedioyle
Hazmat
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Product Information

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Synonyms
Dichlorure de butanedioyle
CAS Number
543-20-4
Purity
≥ 95 % (dosage par titration)
Molecular Formula
C4H4Cl2O2
Molecular Weight
154.97
MDL Number
MFCD00000749
PubChem ID
10970
Melting Point
13 - 15 °C
Density
1.370
Appearance
Poudre blanche ou incolore à orange clair à jaune, en grumeaux ou liquide clair
Boiling Point
191 - 193 °C
Refractive Index
1.470
Conditions
Magasin chez RT
General Information
Synonyms
Dichlorure de butanedioyle
CAS Number
543-20-4
Purity
≥ 95 % (dosage par titration)
Molecular Formula
C4H4Cl2O2
Molecular Weight
154.97
MDL Number
MFCD00000749
PubChem ID
10970
Melting Point
13 - 15 °C
Density
1.370
Appearance
Poudre blanche ou incolore à orange clair à jaune, en grumeaux ou liquide clair
Boiling Point
191 - 193 °C
Refractive Index
1.470
Conditions
Magasin chez RT
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Oui
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Succinyl chloride is widely utilized in research focused on:

  • Synthesis of Peptides: It serves as a key reagent in the synthesis of peptides and proteins, facilitating the formation of amide bonds, which are essential for building these biomolecules.
  • Pharmaceutical Development: This compound is important in the pharmaceutical industry for creating active pharmaceutical ingredients (APIs), particularly in the development of drugs that require acylation reactions.
  • Polymer Chemistry: Succinyl chloride is used in the production of various polymers, enhancing properties such as solubility and thermal stability, which are crucial for applications in coatings and adhesives.
  • Modification of Surfaces: It is employed to modify surfaces of materials, improving adhesion and compatibility in applications like biomedical devices and sensors.
  • Research in Organic Chemistry: Researchers utilize it to explore reaction mechanisms and develop new synthetic pathways, making it a valuable tool in academic and industrial laboratories.

Citations